Presentations

Eising, E. (2024). Exploring the genetics of stuttering. Talk presented at the NCCR Symposium "From Genes to Communication". Geneva. 2024-06-10 - 2024-06-11.

Eising, E., Rebattu, V., Boomsma, D. I., Pool, R., Franken, M.-C.-J., & Fisher, S. E. (2024). Exploring the genetics of stuttering persistence. Poster presented at the 54th Annual Meeting of the Behavior Genetics Association, London.

Eising, E. (2024). Monogenic contributions to speech delay. Talk presented at the CRE Symposium ‘What’s new since FOXP2: new developments in speech and language neurobiology’. London. 2024-06-07.

Eising, E. (2024). Exploring the genetics of stuttering persistence. Talk presented at the Symposium “Speech and Language Disorders: Lessons from Genetics”. Nijmegen, The Netherlands. 2024-09-13.

De Heus, E. V., Eising, E., Fisher, S. E., de Jong, P. F., & Van Bergen, E. (2024). Disentangling dyslexia: Towards early identification through biological and non-biological factors. Poster presented at the 54th Annual Meeting of the Behavior Genetics Association, London.

De Heus, E., Eising, E., Fisher, S. E., De Jong, P. F., & Van Bergen, E. (2024). Disentangling dyslexia: towards early identification through biological and non-biological factors. Poster presented at the Highlights in the Language Sciences Conference 2024, Nijmegen, The Netherlands.

Molz, B., Lana Alberro, M., Eising, E., Schijven, D., Francks, C., & Fisher, S. E. (2024). Evolutionary insights from a population database: Limited consequences of archaic protein-altering variants in present-day humans. Poster presented at the 57th Annual European Human Genetics Conference (ESHG 2024), Berlin, Germany.

Szilagyi, I. A., Vino, A., De boer, J., Eising, E., Hintz, F., Meyer, A. S., & Fisher, S. E. (2024). Polygenic profile of individual differences in language skills in a Dutch cohort. Poster presented at the Highlights in the Language Sciences Conference 2024, Nijmegen, The Netherlands.

Doust, C., Fontanillas, P., Eising, E., Gordon, S. D., GenLang Consortium, Martin, N. G., Bates, T. C., Fisher, S. E., & Luciano, M. (2020). Discovery of genome-wide significant risk loci for dyslexia. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.

Eising, E., St Pourcain, B., Francks, C., Fisher, S. E., & the Quantitative Trait Working Group of the GenLang consortium (2019). A genome-wide association screen of quantitative www.genlang.org speech, language and reading traits in >18,000 people in the GenLang consortium. Poster presented at Cognomics conference, Nijmegen.

Eising, E., St Pourcain, B., Francks, C., & Fisher, S. E. (2020). A GWAS meta-analysis of quantitative reading and language traits in >33,000 people in the GenLang consortium. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.

Eising, E., Niarchou, M., 23andMe Research Team, GenLang QTL-GWAS Working Group, Davis, L., Fisher, S. E., & Gordon, R. (2020). Novel investigation of pleiotropy of rhythm and language traits. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.

Lyu, B., Tsvetanov, K., Tyler, L., Clarke, A., Eising, E., Fisher, S. E., & Amos, W. (2020). Pattern-based genome-wide relatedness analysis of human brain structure. Poster presented at the 27th Annual Meeting of the Cognitive Neuroscience Society (CNS 2020), online.